Version: 8.0.0
Date: Tue Jan 28 2025
optic atrophy 12
DOID:0080840
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

optic atrophy 12

Definition
An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11.
Synonyms
None
Cross References
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Sources of Associations

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      Associated Models

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